Evidence map›Paper›PMID 38613483›Full record

ArticleACS biomaterials science & engineering2024

Liposomal Phenylephrine Nanoparticles Enhance the Antitumor Activity of Intratumoral Chemotherapy in a Preclinical Model of Melanoma.

Emmanuel M Gabriel, Deborah Bahr, Hari Krishnareddy Rachamala, Vijay S Madamsetty, Barath Shreeder, Sanjay Bagaria, Amber L Escobedo, Joel M Reid, Debabrata Mukhopadhyay

Open access · greenAbstract read
In one paragraph

Article in ACS biomaterials science & engineering, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 46% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Emmanuel M GabrielDepartment of Surgery, Division of Surgical Oncology, Mayo Clinic, Jacksonville, Florida 32224, United States.ORCID 0000-0001-8570-4784
Deborah BahrDepartment of Molecular Biology, Mayo Clinic, Jacksonville, Florida 32224, United States.
Hari Krishnareddy RachamalaDepartment of Molecular Biology, Mayo Clinic, Jacksonville, Florida 32224, United States.
Vijay S MadamsettyDepartment of Molecular Biology, Mayo Clinic, Jacksonville, Florida 32224, United States.ORCID 0000-0001-9883-190X
Barath ShreederDepartment of Immunology, Mayo Clinic, Jacksonville, Florida 32224, United States.
Sanjay BagariaDepartment of Surgery, Division of Surgical Oncology, Mayo Clinic, Jacksonville, Florida 32224, United States.
Amber L EscobedoDepartment of Pharmacology, Mayo Clinic, Rochester, Minnesota 55902, United States.
Joel M ReidDepartment of Pharmacology, Mayo Clinic, Rochester, Minnesota 55902, United States.
Debabrata MukhopadhyayDepartment of Molecular Biology, Mayo Clinic, Jacksonville, Florida 32224, United States.ORCID 0000-0003-1858-5054
Mayo Clinic in Florida · USMayo Clinic · US

Funding

Women's Cancer ProgramP30CA015083 · NCI · MAYO CLINIC ROCHESTER · PI AKHILESH PANDEY · 1985 to 2026
$151.3M
Institutional Career Development CoreKL2TR002379 · NCATS · MAYO CLINIC ROCHESTER · PI NILUFER ERTEKIN-TANER · 2017 to 2026
$14.9M
NCATS NIH HHS KL2 TR002379NCI NIH HHS P30 CA015083
6 · The paper itself

Abstract

Intratumoral injection of anticancer agents has limited efficacy and is not routinely used for most cancers. In this study, we aimed to improve the efficacy of intratumoral chemotherapy using a novel approach comprising peri-tumoral injection of sustained-release liposomal nanoparticles containing phenylephrine, which is a potent vasoconstrictor. Using a preclinical model of melanoma, we have previously shown that systemically administered (intravenous) phenylephrine could transiently shunt blood flow to the tumor at the time of drug delivery, which in turn improved antitumor responses. This approach was called dynamic control of tumor-associated vessels. Herein, we used liposomal phenylephrine nanoparticles as a "local" dynamic control strategy for the B16 melanoma. Local dynamic control was shown to increase the retention and exposure time of tumors to intratumorally injected chemotherapy (melphalan). C57BL/6 mice bearing B16 tumors were treated with intratumoral melphalan and peri-tumoral injection of sustained-release liposomal phenylephrine nanoparticles (i.e., the local dynamic control protocol). These mice had statistically significantly improved antitumor responses compared to melphalan alone (

Indexed as

LiposomesMelanoma, ExperimentalMice, Inbred C57BLNanoparticlesPhenylephrineAnimalsAntineoplastic AgentsCell Line, TumorMelanomaMelphalanMiceAntineoplastic AgentsLiposomesMelphalanPhenylephrinecancer therapiesdrug deliverytumor vessels

Identifiers

PMID38613483
PMCPMC11301277
OpenAlexW4394786707

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.